Shen Hong, Li Rui, Xiao Hong, Zhou Qun, Cui Qing, Chen Jianfang
Neuro-psychiatric Institute, Nanjing Brain Hospital Affiliated to Nanjing Medical University, 264 Guangzhou Road, Nanjing 210029, China.
J Psychiatr Res. 2009 Mar;43(6):615-9. doi: 10.1016/j.jpsychires.2008.09.009. Epub 2008 Oct 30.
This study was to evaluate the relationship between clozapine and aPL in schizophrenia patients.
163 Participants were evaluated: 37 unmedicated schizophrenia patients, 50 clozapine-treated schizophrenia patients and 76 age- and sex-matched healthy controls. A fasting blood sample was taken for serum aPL and serum clozapine level. Serum aPL were measured by ELISA technique and HPLC method was used for the determination of serum clozapine level.
The unmedicated schizophrenia patients showed higher IgG aCL level [mean+/-SD: 1.51+/-0.81 and 1.25+/-0.13 U, respectively (t=2.77, df=111, p<0.01)] and IgM aCL level [mean+/-SD: 1.53+/-0.54. and 1.33+/-0.15 U, respectively (t=-2.98, df=111, p<0.01)] compared with the healthy controls. The comparison of the clozapine-treated schizophrenia patients and the healthy controls showed significant difference in IgG aCL level [mean+/-SD: 1.74+/-0.90 and 1.25+/-0.13 U, respectively (t=-4.77, df=124, p<0.01)] and IgM aCL level [mean+/-SD: 1.62+/-0.83 and 1.33+/-0.15 U, respectively (t=-4.35, df=124, p<0.01)]. In clozapine-treated schizophrenia patients, the results of Pearson correlation coefficients showed that there was a significant positive relationship between serum IgM aCL and serum clozapine level (r=0.461, p<0.01), and serum IgG aCL were significantly correlated with serum IgM aCL (r=0.279, p<0.05). Stepwise multiple regression analysis was performed with various characteristics, such as duration of medication, daily dose and serum clozapine level as candidate factors for serum aCL (IgG and IgM isotypes) in clozapine-treated schizophrenia patients. Only serum clozapine level was able to enter into the regression model of IgM aCL (Model R(2)=0.212, p<0.05).
A higher serum clozapine level is associated with an increased aPL in schizophrenia patients.
本研究旨在评估氯氮平与精神分裂症患者抗磷脂抗体(aPL)之间的关系。
对163名参与者进行了评估:37名未接受药物治疗的精神分裂症患者、50名接受氯氮平治疗的精神分裂症患者以及76名年龄和性别匹配的健康对照者。采集空腹血样以检测血清aPL和血清氯氮平水平。血清aPL采用酶联免疫吸附测定(ELISA)技术进行检测,血清氯氮平水平采用高效液相色谱(HPLC)法进行测定。
与健康对照者相比,未接受药物治疗的精神分裂症患者的IgG型抗心磷脂抗体(aCL)水平[平均值±标准差:分别为1.51±0.81和1.25±0.13 U(t = 2.77,自由度 = 111,p < 0.01)]和IgM型aCL水平[平均值±标准差:分别为1.53±0.54和1.33±0.15 U(t = -2.98,自由度 = 111,p < 0.01)]更高。接受氯氮平治疗的精神分裂症患者与健康对照者相比,IgG型aCL水平[平均值±标准差:分别为1.74±0.90和1.25±0.13 U(t = -4.77,自由度 = 124,p < 0.01)]和IgM型aCL水平[平均值±标准差:分别为1.62±0.83和1.33±0.15 U(t = -4.35,自由度 = 直,p < 0.01)]存在显著差异。在接受氯氮平治疗的精神分裂症患者中,Pearson相关系数结果显示血清IgM型aCL与血清氯氮平水平之间存在显著正相关(r = 0.461,p < 0.01),血清IgG型aCL与血清IgM型aCL显著相关(r = 0.279,p < 0.05)。对接受氯氮平治疗的精神分裂症患者,以用药时长、每日剂量和血清氯氮平水平等各种特征作为血清aCL(IgG和IgM亚型)的候选因素进行逐步多元回归分析。只有血清氯氮平水平能够进入IgMaCL的回归模型(模型R² = 0.212,p < 0.05)。
精神分裂症患者血清氯氮平水平较高与aPL增加有关。